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Size-Controlled Synthesis of Granular Polyphosphate Nanoparticles at Physiologic Salt Concentrations for Blood Clotting

机译:生理盐浓度用于血凝块的大小受控的多聚磷酸盐纳米颗粒的合成。

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Size-controlled granular polyphosphate (PolyP) nanoparticles were synthesized by precipitation in aqueous solutions containing physiological concentrations of calcium and magnesium. We demonstrate using dynamic light scattering (DLS) that the solubility is correlated inversely with PolyP chain length, with very long chain PolyP (PolyP 1000+, more than 1000 repeating units) normally found in prokaryotes precipitating much more robustly than shorter chains like those found in human platelet dense granules (PolyP80, range 76—84 repeating units). It is believed that the precipitation of PolyP is a reversible process involving calcium coordination to phosphate monomers in the polymer chain. The particles are stable in aqueous buffer and albumin suspensions on time scales roughly equivalent to catastrophic bleeding events. Transmission electron microscopy images demonstrate that the PolyP nanoparticles are spherical and uniformly electron dense, with a particle diameter of 200—250 nm, closely resembling the content of acidocalcisom.es. X-ray elemental analysis further reveals that the P/Ca ratio is 67:32. The granular nanoparticles also manifest promising procoagulant effects, as measured by in vitro clotting tests assaying contact pathway activity.
机译:通过在含有生理浓度的钙和镁的水溶液中沉淀来合成尺寸受控的颗粒状多磷酸盐(PolyP)纳米颗粒。我们使用动态光散射(DLS)证明了溶解度与PolyP链长成反比,通常在原核生物中发现很长的链PolyP(PolyP 1000+,超过1000个重复单元)比短链更牢固地沉淀。在人类血小板致密颗粒中(PolyP80,范围76-84重复单位)。据信,PolyP的沉淀是可逆的过程,涉及钙与聚合物链中的磷酸酯单体配位。颗粒在水性缓冲液和白蛋白悬浮液中稳定,时间尺度大致相当于灾难性出血事件。透射电子显微镜图像表明,PolyP纳米颗粒是球形的,并且具有均匀的电子致密性,粒径为200-250 nm,非常类似于酸性降钙素的含量。 X射线元素分析进一步揭示P / Ca比为67:32。如通过测定接触途径活性的体外凝结试验所测量的,颗粒状纳米颗粒还显示出有希望的促凝作用。

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